Canonical Allele Identifier: CA913171797
Gene:

Linked Data

ClinVar Variation Id: 1684911
ClinVar RCV Id: RCV002248003
dbSNP Id: rs2124598415
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14680C>A , J01415.2:m.14680C>A GRCh38
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